Full-thickness Skin Grafts for Hand Contractures in an Adult Patient with Junctional Epidermolysis Bullosa: A Case Report.

Sayaka Nakamura, Susumu Saito, Yoshihiro Ishida, Yo Kaku, Ken Natsuga, Naoki Morimoto
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Abstract

Epidermolysis bullosa is a group of inherited skin fragility disorders with blister formation in the basement membrane zone. Chronic scarring after repeated blistering of the hands causes narrowing of the first web, flexion contractures of the digits, and pseudosyndactyly. Junctional epidermolysis bullosa is a type of epidermolysis bullosa that is characterized by blister formation in the lamina lucida. This condition is associated with survival into adulthood. In adult survivors, hand function might be required in order to participate in normal social activities. However, there is a lack of literature on the management of hand surgery for adult patients with junctional epidermolysis bullosa. We herein describe an adult patient with junctional epidermolysis bullosa who had pseudosyndactyly and flexion contractures in both hands. Five surgeries were performed. Contractures were released and reconstructed using split- or full-thickness skin grafts. Delayed wound healing was always observed due to epidermal necrosis in the graft. After epithelialization, a satisfactory functional outcome was obtained.

全层皮肤移植治疗成年大疱性结缔组织表皮松解症手部挛缩1例。
大疱性表皮松解症是一组遗传性皮肤脆性疾病,在基底膜区形成水疱。手部反复起泡后的慢性瘢痕导致第一蹼狭窄,手指屈曲挛缩和假性并指。交界性大疱性表皮松解症是一种大疱性表皮松解症,其特征是在透明层形成水疱。这种情况与能否存活到成年有关。在成年幸存者中,为了参与正常的社会活动,手部功能可能是必需的。然而,对于成年大疱性结膜表皮松解症患者的手部手术治疗,目前还缺乏相关文献。我们在此描述了一个成年患者的结缔性表皮松解症谁有假性并指和屈曲挛缩在双手。共进行了5次手术。挛缩被释放,并使用分裂或全层皮肤移植重建。由于移植物表皮坏死,经常观察到伤口愈合延迟。上皮化后,获得了令人满意的功能结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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